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About

CIMS Global provides regulated data science platforms and eClinical solutions designed to reshape the future of clinical trials by improving the quality, efficiency, and speed of clinical trial data acquisition, processing, analysis, monitoring, and regulatory submission. Its suite includes innovative solutions such as CRE, DDM, DMC-HUB, and eBinder, along with an eClinical Suite that supports data collection, analytics, and clinical applications across every step of a trial. CRE is a multi-tenant, validated Statistical Computing Environment for compliant clinical data analysis, using R, RShiny, and the RStudio IDE within a secure, audit-ready framework that meets 21 CFR Part 11 and GxP standards. DDM is a patented Dynamic Data Monitoring platform that displays cumulative treatment effect on a trial radar screen and predicts a clinical trial’s chance of success or failure.

About

eCOA by EvidentIQ optimizes real-time, direct-from-patient data collection by offering a simple and intuitive interface providing advanced patient assessments to enhance the patient experience and improve data quality. Customers can benefit from an end-to-end comprehensive eCOA package or create value by selecting from the various elements meeting specific requirements. Book a demo with our team of experts and see how you can improve your study ROI. eCOA by EvidentIQ brings data science services and technology together. Customers can benefit from an end-to-end comprehensive eCOA package or create value by selecting various elements meeting specific requirements. The solution can be used stand-alone as it is independent of any specific eClinical technologies such as EDC systems, but it can be integrated in any existing eClinical software landscape. It has been created to collect any patient/clinician/observer reported outcome data in a streamlined, compliant and efficient way.

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Audience

Clinical trial sponsors, CROs, and data monitoring committees that need regulated data science tools, eClinical systems, and AI-powered monitoring to optimize trials and improve decision-making

Audience

Healthcare providers interested in a clinical trial management solution to optimize their data collection processes

Support

Phone Support
24/7 Live Support
Online

Support

Phone Support
24/7 Live Support
Online

API

Offers API

API

Offers API

Screenshots and Videos

Screenshots and Videos

Pricing

No information available.
Free Version
Free Trial

Pricing

No information available.
Free Version
Free Trial

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Training

Documentation
Webinars
Live Online
In Person

Training

Documentation
Webinars
Live Online
In Person

Company Information

CIMS Global
Founded: 2004
United States
cims-global.com

Company Information

EvidentIQ
Germany
www.evidentiq.com

Alternatives

Alternatives

Clinion eCOA

Clinion eCOA

Clinion
TrialKit

TrialKit

Crucial Data Solutions
MainEDC

MainEDC

Data Management 365
Clario eCOA

Clario eCOA

Clario

Categories

Categories

Clinical Trial Management Features

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

Electronic Data Capture Features

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management

Integrations

R
RStudio

Integrations

R
RStudio
Claim CIMS Global and update features and information
Claim CIMS Global and update features and information
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